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Volumn 12, Issue 6, 2010, Pages 1256-1259

Diastereoselective allylstannane additions to (S)-5,6-dihydro-2H-5- phenyloxazin-2-one. A concise synthesis of (S)-β-methylisoleucine

Author keywords

[No Author keywords available]

Indexed keywords

5,6 DIHYDRO 2H 5 PHENYLOXAZIN 2 ONE; 5,6-DIHYDRO-2H-5-PHENYLOXAZIN-2-ONE; BETA METHYLISOLEUCINE; BETA-METHYLISOLEUCINE; DRUG DERIVATIVE; G PROTEIN COUPLED RECEPTOR; ISOLEUCINE; OXAZINE DERIVATIVE; STANNANE; TIN DERIVATIVE;

EID: 77949811756     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1001126     Document Type: Article
Times cited : (7)

References (35)
  • 8
    • 0022927999 scopus 로고
    • Curiously, the first identification of naturally occurring 1b was from an extraterrestrial source: the Murchison meteorite, a carbonaceous chondrite
    • Curiously, the first identification of naturally occurring 1b was from an extraterrestrial source: the Murchison meteorite, a carbonaceous chondrite. Cronin, J. R.; Pizzarello, S. Geochim. Cosmochim. Acta 1986, 50, 2419.
    • (1986) Geochim. Cosmochim. Acta , vol.50 , pp. 2419
    • Cronin, J.R.1    Pizzarello, S.2
  • 20
    • 0001459021 scopus 로고
    • The 5,6-diphenylmorpholinone 3a has been used both as a nucleophilic glycine equivalent and precursor for in situ prepartion of the electrophilic 3b (a)
    • The 5,6-diphenylmorpholinone 3a has been used both as a nucleophilic glycine equivalent and precursor for in situ prepartion of the electrophilic 3b. (a) Williams, R. M. Aldrichim. Acta 1992, 25, 11.
    • (1992) Aldrichim. Acta , vol.25 , pp. 11
    • Williams, R.M.1
  • 21
    • 0001122927 scopus 로고
    • and references cited therein.
    • (b) Williams, R. M.; Hendrix, J. A. Chem. Rev. 1992, 92, 889, and references cited therein.
    • (1992) Chem. Rev. , vol.92 , pp. 889
    • Williams, R.M.1    Hendrix, J.A.2
  • 22
    • 33845278130 scopus 로고
    • 3b and 3c have been converted to arylglycines by Mannich reaction with arenes
    • Williams, R. M.; Sinclair, P. J.; Zhai, D.; Chen, D. J. Am. Chem. Soc. 1988, 110, 1547. 3b and 3c have been converted to arylglycines by Mannich reaction with arenes.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 1547
    • Williams, R.M.1    Sinclair, P.J.2    Zhai, D.3    Chen, D.4
  • 24
    • 0042831486 scopus 로고    scopus 로고
    • 3b,c were made in 5-6 steps from phenylglycine, and 3a from benzoin
    • (e) Chen, Y.-J.; Lei, F.; Liu, L.; Wang, D. Tetrahedron 2003, 59, 7609. 3b,c were made in 5-6 steps from phenylglycine, and 3a from benzoin.
    • (2003) Tetrahedron , vol.59 , pp. 7609
    • Chen, Y.-J.1    Lei, F.2    Liu, L.3    Wang, D.4
  • 31
    • 77949836717 scopus 로고    scopus 로고
    • 10,12 and conversion of 4b to (S)-1b
    • 10,12 and conversion of 4b to (S)-1b.
  • 32
    • 77949835232 scopus 로고    scopus 로고
    • Side-product formation led to diminished yields of the desired 4a
    • Side-product formation led to diminished yields of the desired 4a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.